FDA 510(k)
Unknown
🇺🇸 United States
SUGITA ANEURYSM CLIPS, APPLIERS & CASE
K Number: K791978
·
Decision Sep 28, 1979
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
152
Review Days
—
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Basic Information
- Device Name
- SUGITA ANEURYSM CLIPS, APPLIERS & CASE
- K Number
- K791978
- Clearance Type
- Traditional
- Decision
- Unknown
- Applicant
- Codman & Shurtleff, Inc.
- Date Received
- September 28, 1979
- Decision Date
- September 28, 1979
- Advisory Committee
- Unknown
- Review Advisory Committee
- NE
- Third Party
- N
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